Anti-microbial composition

a technology of composition and antimicrobial, applied in the field of antimicrobial, can solve the problems of bacteria having drug resistance, becoming a major health problem, expensive, etc., and achieve the effect of increasing the effect and/or the scope of the antiobitic, and increasing the effect and/or the scope of the active blend of the invention

Active Publication Date: 2013-10-31
SEPTEOS
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0145]It has been surprisingly discovered that the active blend of the invention is able to potentiate the antibiotics, advantageously meaning that the effect and / or the scope of the antiobitic is increased. Furthermore, the combination active blend of the invention plus antibiotic can be efficient against bacteria which are resistant to the antibiotic of the combination. Thus, the active blend of the invention can be used to re-sensibilize bacteria towards antiobiotic
[0146]It has been surprisingly discovered that the antibiotics is able to potentiate the active blend of the invention, advantageously meaning that the effect and / or the scope of the active blend of the invention is increased.
[0147]The synergy effect is particularly observed with antibiotics with other target than the membrane (gentamicin, amikacin, erythromycin and clindamycin).

Problems solved by technology

For example in the case of bacteria it becomes a major problem to find novel efficient anti-bacterial compositions to prevent or treat bacterial infections.
Apparition and propagation of microbial strains resistant to almost all or even to all the known anti-microbial agents becomes a major health issue.
Known anti-microbial agents may exhibit the following drawbacks they may have an insufficient activity, in particular at low level and / or when interfering agent are present, they may be insufficiently active or not active at all on some or on any drug resistant microbes, in particular on drug resistant bacteria such as drug resistant Staphylococcus aureus, for example such as MRSA, VRSA; drug resistant enterobacter, such as NDM-1, or New Dehli Metallo-beta-lactamase type 1; they may presenting undesirable side effects, they may not be well tolerated by the organism, their use may lead to bacteria having drug resistance, in particular crossed drug resistance, they may be expensive, and / or difficult to obtain.
More particularly cinnamon essential oils, especially those comprising trans-cinnamaldehyde, or trans-cinnamaldehyde alone are known to be a potent anti-microbial, however, they lead to undesirable effects, such as neurotoxicity, which may lead to death in case of high dose, hepatotoxicity, irritation of the skin, sensitization of the skin, phototoxicity and / or photoallergy.

Method used

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Examples

Experimental program
Comparison scheme
Effect test

example 1

Bacterial Strains

[0308]The tested strains have been isolated from various samplings from human patients (blood, urines, pulmonary aspiration, etc). They have been isolated from patients non-infected at their admission to the hospital and who have developed an infection after at least 48 h of hospitalisation. The studied strains are as follows:

TABLE 1Enterobacteriaceaen = 89Citrobacter freundiiPhenotypic characterisation: Cephalosporinase, WSBL, WildGenotypic characterisation: CTX M1, CTX M15, KPC-2, NDM-1,TEM 3Enterobacter cloacaePhenotypic characterisation: Cephalosporinase (HN2), WSBL, WildGenotypic characterisation: GES-, KPC-2, NDM-1, NMC-A, OXA-43Escherichia coliPhenotypic characterisation: WSBL, Wild, Penicilinases,Fluoroquinolone resistance, Nalixidic acid resistanceGenotypic characterisation: CMY.2, CTX M1, CTX M14, CTX M15,CTX M3, KPC-2, NDM-1, OXA-30, OXA-48, SHV-12, SHV-2A,TEM-12, VIM-1, VIM-19, VIM-2Klebsiella pneumoniaePhenotypic characterisation: Penicillinase, wildGen...

example 2

Antibacterial Activity of Blend 1

[0309]Following a method allowing the dissolution of the active blend in a Mueller Hinton gelose the following MIC has been measured with the following active blend 1 consisting of 1% by weight of cineole, 2.4% by weight of linalool, 1.7% by weight of beta-caryophyllene, 86.7% by weight of trans-cinnamaldehyde, 5.35% by weight of trans-2-methoxycinnamaldehyde, 0.35% by weight of benzyl benzoate, and 2.5% by weight of cinnamyl acetate compared to the total weight of the active blend. Said active blend 1 having been tested at concentrations shown in the following table.

TABLE 2MICMICStrainType(% v / v)StrainType(% v / v)ATCC 25922E. coli0.038241Staphylococcus0.038127Pseudomonas0.1258152Enterococcus0.038128Pseudomonas0.1258153Enterococcus0.038129Pseudomonas0.1259001E. faecium0.038130Pseudomonas0.1259002E. faecium0.038131Pseudomonas0.039003E. coli0.038132Pseudomonas0.1259004E. aerogenes0.038133Pseudomonas0.1259007P. aeruginosa0.068134Pseudomonas0.1259008P. ae...

example 3

Antibacterial Activity of Active Blends 2, 3, 4 and 5

[0311]Following a method allowing the dissolution of the active blend in a Mueller Hinton gelose the following MIC has been measured with the following active blends:[0312]Active blend 2 consisting of 2.4% by weight of linalool, 1.72% by weight of beta-caryophyllene, 87.58% by weight of trans-cinnamaldehyde, 5.43% by weight of trans-2-methoxycinnamaldehyde, 0.34% by weight of benzyl benzoate, and 2.53% by weight of cinnamyl acetate compared to the total weight of the active blend, and[0313]Active blend 3 consisting of 1.04% by weight of cineole, 2.42% by weight of linalool, 88.19% by weight of tran s-cinnamaldehyde, 5.47% by weight of trans-2-methoxycinnamaldehyde, 0.35% by weight of benzyl benzoate, and 2.54% by weight of cinnamyl acetate compared to the total weight of the active blend,[0314]active blend 4 consisting of 2.41% by weight of linalool, 1.72% by weight of beta-caryophyllene, 87.88% by weight of trans-cinnamaldehyde, ...

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Abstract

This invention pertains to an anti-microbial, in particular anti-bacterial and/or anti-fungal composition comprising cinnamaldehyde, trans-2-methoxy cinnamaldehyde, cinnamyl acetate and linalool. In particular this composition is intended for preventing and/or treating microbial infection in an animal.

Description

[0001]This invention pertains to an anti-microbial, in particular anti-bacterial, more particularly against Gram− bacteria, and / or anti-fungal and / or anti-viral composition comprising cinnamaldehyde, trans-2-methoxycinnamaldehyde, cinnamyl acetate and linalool. In particular this composition is intended for preventing and / or treating microbial infection in an animal.[0002]The arrival of penicillin followed by streptomycin in the 40s opened the era of anti-bacterials. The discovery of anti-bacterial compounds such as penicillin, aminosides, macrolides and quinolones have been one of the biggest achievement of the modern medicine for the treatment of bacterial infections.[0003]However, there is a growing need for new compounds or compositions allowing fighting bacterial infections. This need is in particular due to the fact that there is more and more microbes which are exhibiting various drug resistance to known anti-microbial compounds or compositions.[0004]For example in the case o...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): A61K31/015A61K31/235A61K31/045A61K45/06A61K31/35A61K31/11
CPCA61K31/015A61K31/35A61K31/11A61K31/045A61K45/06A61K31/235A61K9/0014A61K9/0019A61K31/04A61K31/08A61K31/22A61K31/37A61K47/10A61K47/32A61K31/352A61P31/04A61P31/10Y02A50/30A61K2300/00A01N65/24A61P1/04A61K36/54A01N35/02A61K31/222
Inventor TESSE, NICOLAS
Owner SEPTEOS
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